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Research 91–120 of 1000+
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- The Genetics of Human Skin Disease
- Keratins: the hair shaft's backbone revealed
- Keratin gene mutations in disorders of human skin and its appendages
- The molecular basis of human keratin disorders
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Commentary
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets in a Pomeranian Dog Caused by a Novel Mutation in the Vitamin D Receptor Gene
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Skin Development and Disease: A Molecular Perspective
- Directed Expression of a Chimeric Type II Keratin Partially Rescues Keratin 5-null Mice
- The Study on Biological Function of Keratin 26, a Novel Member of Liaoning Cashmere Goat Keratin Gene Family
- Cornified Epithelial Teeth of Jawless Vertebrates Contain Proteins Similar to Keratin-Associated Proteins of Mammalian Skin Appendages
- Cannabinoid Compounds as a Pharmacotherapeutic Option for the Treatment of Non-Cancer Skin Diseases
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Isolation and Characterization of a Putative Keratin-Associated Protein Gene Expressed in Embryonic Skin of Mice
- Connexin mutations in human disease
- Frontal fibrosing alopecia: A review of disease pathogenesis
- Frizzled Receptors in Development and Disease
- Mechanical forces in skin disorders
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- What Ages Hair?
- New small molecules in dermatology: for the autoimmunity, inflammation and beyond
- Comprehensive RNA sequencing in primary murine keratinocytes and fibroblasts identifies novel biomarkers and provides potential therapeutic targets for skin-related diseases